[18F]MK-9470, a positron emission tomography (PET) tracer for in vivo human PET brain imaging of the cannabinoid-1 receptor

被引:242
作者
Burns, H. Donald
Van Laere, Koen
Sanabria-Bohorquez, Sandra
Hamill, Terence G.
Bormans, Guy
Eng, Wai-si
Gibson, Ray
Ryan, Christine
Connolly, Brett
Patel, Shil
Krause, Stephen
Vanko, Amy
Van Hecken, Anne
Dupont, Patrick
De Lepeleire, Inge
Rothenberg, Paul
Stoch, S. Aubrey
Cote, Josee
Hagmann, William K.
Jewell, James P.
Lin, Linus S.
Liu, Ping
Goulet, Mark T.
Gottesdiener, Keith
Wagner, John A.
de Hoon, Jan
Mortelmans, Luc
Fong, Tung M.
Hargreaves, Richard J.
机构
[1] Merck Res Labs, Nucl Imaging Res, West Point, PA 19486 USA
[2] Katholieke Univ Leuven, Lab Radiopharm, B-3000 Louvain, Belgium
[3] Univ Hosp, Div Nucl Med, B-3000 Louvain, Belgium
[4] Katholieke Univ Leuven, Ctr Clin Pharmacol, B-3000 Louvain, Belgium
[5] Merck Res Labs, B-1180 Brussels, Belgium
[6] Merck Res Labs, Metabol Disorders, Rahway, NJ 07065 USA
[7] Merck Res Labs, Med Chem, Rahway, NJ 07065 USA
[8] Merck Res Labs, Clin Pharmacol, Upper Gwynedd, PA 19454 USA
关键词
inverse agonist occupancy;
D O I
10.1073/pnas.0703472104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
[F-18]MK-9470 is a selective, high-affinity, inverse agonist (human IC50,0.7 nM)for the cannabinoid CB1 receptor (CB1 R) that has been developed for use in human brain imaging. Autoradiographic studies in rhesus monkey brain showed that [F-18]MK-9470 binding is aligned with the reported distribution of CB1 receptors with high specific binding in the cerebral cortex, cerebellum, cauclate/putamen, globus pallidus, substantia nigra, and hippocampus. Positron emission tomography (PET) imaging studies in rhesus monkeys showed high brain uptake and a distribution pattern generally consistent with that seen in the autoradiographic studies. Uptake was blocked by pretreatment with a potent CB1 inverse agonist, MK-0364. The ratio of total to nonspecific binding in putamen was 4-5:1, indicative of a strong specific signal that was confirmed to be reversible via displacement studies with MK-0364. Baseline PET imaging studies in human research subject demonstrated behavior of [F-18]MK-9470 very similar to that seen in monkeys, with very good test-retest variability (7%). Proof of concept studies in healthy young male human subjects showed that MK-0364, given orally, produced a dose-related reduction in [F-18]MK-9470 binding reflecting CB1R receptor occupancy by the drug. Thus, [F-18]MK-9470 has the potential to be a valuable, noninvasive research tool for the in vivo study of CB1R biology and pharmacology in a variety of neuropsychiatric disorders in humans. In addition, it allows demonstration of target engagement and noninvasive close-occupancy studies to aid in dose selection for clinical trials of CB1R inverse agonists.
引用
收藏
页码:9800 / 9805
页数:6
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